Canonical Allele Identifier: CA2309139649
Gene: LINC01924 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.64209947C= , CM000680.2:g.64209947C= GRCh38
NC_000018.9:g.61877182C= , CM000680.1:g.61877182C= GRCh37
NC_000018.8:g.60028162C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033881.1:n.201-39354C=